Glass composition for producing high strength and high modulus fibers

ABSTRACT

A glass composition including SiO 2  in an amount from 60.0 to 73.01% by weight, Al 2 O 3  in an amount from about 13.0 to about 26.0% by weight, MgO in an amount from about 5.0 to about 12.75% by weight, CaO in an amount from about 3.25 to about 4.0% by weight, Li 2 O in an amount from about 3.25 to about 4.0% by weight, and Na 2 O in an amount from 0.0 to about 0.75% by weight is provided. Glass fibers formed from the inventive composition may be used in applications that require high strength, high stiffness, and low weight. Such applications include, but are not limited to, woven fabrics for use in forming wind blades, armor plating, and aerospace structures.

CROSS REFERENCE TO RELATED APPLICATION

This application is the U.S. national phase entry of PCT/IB11/052899 with an international filing date of Jun. 30, 2011 which claims priority and all other benefits of U.S. Provisional Application Ser. No. 61/360,138 both of which are hereby incorporated by reference in their entirety.

TECHNICAL FIELD AND INDUSTRIAL APPLICABILITY

The present invention relates generally to a glass composition, and more particularly, to a high performance glass composition that possesses acceptable forming properties and whose components are melted in a refractory melter. Glass fibers formed from the inventive composition possess high strength and improved modulus and may be used to reinforce composite matrices where high strength and light weight are desired.

BACKGROUND

Glass fibers are manufactured from various raw materials combined in specific proportions to yield a desired chemical composition. This collection of materials is commonly termed a “glass batch.” To form glass fibers, typically the glass batch is melted in a melter or melting apparatus, the molten glass is drawn into filaments through a bushing or orifice plate, and a sizing composition containing lubricants, coupling agents, and film-forming binder resins is applied to the filaments. After the sizing is applied, the fibers may be gathered into one or more strands and wound into a package or, alternatively, the fibers may be chopped while wet and collected. The collected chopped strands may then be dried and cured to form dry chopped fibers or they can be packaged in their wet condition as wet chopped fibers.

The composition of the glass batch and the glass manufactured from it are typically expressed in terms of percentages of the components, which are mainly expressed as oxides. SiO₂, Al₂O₃, CaO, MgO, B₂O₃, Na₂O, K₂O, Fe₂O₃, and minor amounts of other compounds such as TiO₂, Li₂O, BaO, SrO, ZnO, ZrO₂, P₂O₅, fluorine, and SO₃ are common components of a glass batch. Numerous types of glasses may be produced from varying the amounts of these oxides, or eliminating some of the oxides in the glass batch. Examples of such glasses that may be produced include R-glass, E-glass, S-glass, A-glass, C-glass, and ECR-glass. The glass composition controls the forming and product properties of the glass. Other characteristics of glass compositions include the raw material cost and environmental impact.

There is a unique combination of forming properties that permits a glass to be melted and distributed in a conventional refractory tank and glass distribution system. First, the temperature at which the glass is held must be low enough so that it does not aggressively attack the refractory. An attack on a refractory can take place, for example, by exceeding the maximum use temperature of the refractory or by increasing the rate at which the glass corrodes and erodes the refractory to an unacceptably high level. Refractory corrosion rate is strongly increased as the glass becomes more fluid by a decrease in the glass viscosity. Therefore, in order for a glass to be melted in a refractory tank, the temperature of the refractory must be kept below a certain temperature and the glass viscosity (e.g., resistance to flow) must be maintained above a certain value. Also, the temperature of the glass in the melting unit, as well as throughout the entire distribution and fiberizing process, must be high enough to prevent crystallization of the glass (i.e., it must be kept at a temperature above the liquidus temperature).

At the fiberizer, it is common to require a minimum temperature differential between the temperature selected for fiberizing (i.e., forming temperature) and the liquidus temperature of the glass. This temperature differential, ΔT, is a measurement of how easily continuous fibers can be formed without production of the fibers being interrupted by breaks caused from devitrification crystals. Accordingly, it is desirable to have as large a ΔT as possible to achieve continuous and uninterrupted glass fiber formation.

In the quest for glass fibers having a higher end performance, ΔT has, at times, been sacrificed to achieve desired end properties. The consequence of this sacrifice is a requirement that the glass be melted in a platinum or platinum-alloy lined furnace, either because the temperature exceeded the maximum end use temperature of the conventional refractory materials or because the viscosity of the glass was such that the temperature of the glass body could not be held above the liquidus temperature while producing a glass viscosity high enough to keep the refractory corrosion at an acceptable level. S2-glass is one example where both of these phenomena take place. The melting temperature of S2-glass is too high for common refractory materials and the ΔT is very small (or negative), thus causing the glass to be very fluid and very corrosive to conventional refractories at glass temperatures above the liquidus temperature. Conventional R-glass also has a very small ΔT, and is therefore melted in platinum or platinum-alloy lined melters.

Thus, there is a need in the art for high-performance glass compositions that retain favorable mechanical and physical properties (e.g., specific modulus and tensile strength) and forming properties (e.g., liquidus temperature and forming temperature) where the forming temperature is sufficiently low and the difference between the forming and liquidus temperatures is large enough to enable the components of the glass composition to be melted in a conventional refractory tank.

SUMMARY

In one embodiment of the invention, a composition that includes SiO₂ in an amount from about 60.0 to about 73.01% by weight, Al₂O₃ in an amount from about 13.0 to about 26.0% by weight, CaO in an amount from 0.0 to about 4.0% by weight, MgO in an amount from about 5.0 to about 12.75% by weight, Li₂O in an amount from about 3.25 to about 4.0% by weight, and Na₂O in an amount from 0.0 to about 0.75% by weight is provided. The phrase “% by weight”, as used herein, is intended to be defined as the percent by weight of the total composition. Additionally, the composition may optionally contain trace quantities of other components or impurities that are not intentionally added. In exemplary embodiments, the glass composition is free or substantially free of B₂O₃ and fluorine, although either can be added in small amounts to adjust the fiberizing and finished glass properties and will not adversely impact the properties if maintained below several percent. As used herein, substantially free of B₂O₃ and fluorine means that the sum of the amounts of B₂O₃ and fluorine present in the composition is less than 1% by weight of the composition. The sum of the amounts of B₂O₃ and fluorine present in the composition can be less than 0.5% by weight of the composition, or less than 0.2% by weight of the composition. Further, the glass composition possesses a forming temperature (also referred to herein as the fiberizing temperature or the log 3 temperature) that is low enough to utilize low cost refractory melters instead of conventional high cost platinum-alloy lined melters in the formation of the glass fibers.

In another embodiment of the present invention, a continuous glass fiber formed of the composition described above is produced using a refractory tank melter. By utilizing a refractory tank formed of refractory blocks, manufacturing costs associated with the production of glass fibers produced by the inventive composition may be reduced. The glass compositions may be used to form continuous glass strands for use in applications where high strength, stiffness, and low density are required.

In yet another embodiment of the present invention, a reinforced composite formed of a product a matrix material and a plurality of fibers formed with the composition described above is provided. The matrix material may be any suitable thermoplastic or thermoset resin known to those of skill in the art, and include thermoplastics such as polyesters, polypropylene, polyimide, polyethylene terephtalate, and polybutylene, and thermoset resins such as epoxy resins, unsaturated polyesters, phenolics, vinylesters, and elastomers. The polymer resins can be used alone or in combination to form the final composite product.

In a further embodiment of the present invention, a method of forming a high performance glass fiber is provided. The fibers may be formed by obtaining the raw ingredients and mixing the components in the appropriate quantities to give the desired weight percentages of the final composition. The mixed batch is then melted in a traditional refractory melter and drawn through orifices of platinum-alloy based bushings to form glass fibers. Strands of glass fibers are formed by gathering the individual filaments together. The strands may be wound and further processed in a conventional manner suitable for the intended application. The glass fibers of the invention are obtainable by any of the methods of forming glass fibers described herein.

In another embodiment of the invention, a reinforced composite product comprising a polymer matrix and a plurality of glass fibers is provided.

In another embodiment of the present invention, glass fibers faulted from the inventive compositions have a liquidus temperature no greater than about 1320° C., a log 3 temperature less than about 1505° C., a ΔT up to about 205° C. In one embodiment, the log 3 temperature can be less than about 1445° C.

In another embodiment of the present invention, glass fibers formed from the inventive compositions have a liquidus temperature no greater than about 1320° C., a log 3 temperature less than about 1500° C., a ΔT up to about 205° C.

In yet another embodiment of the invention, glass fibers formed from the inventive composition have a pristine fiber tensile strength between about 4390 and about 4820 MPa, a modulus between about 82 and about 91 GPa and a density between about 2.39 and 2.52 g/cc.

In yet another embodiment of the invention, glass fibers formed from the inventive composition have a pristine fiber tensile strength between about 4390 and about 4820 MPa, a modulus between about 83 and about 90 GPa, and a density between about 2.39 and 2.52 g/cc.

In a further embodiment of the invention, glass fibers formed from the inventive composition have a specific modulus from about 34.5 MJ/kg to about 35.9 MJ/kg and a specific strength from about 1.8 MJ/kg to about 2.0 MJ/kg.

In another embodiment of the present invention, the glass composition possesses a forming viscosity that is low enough, and a ΔT that is large enough, to utilize low cost refractory melters instead of conventional high cost platinum-alloy lined melters in the formation of the glass fibers.

In another embodiment of the present invention, fibers formed from the inventive composition are formed at a lower cost due to the lower energy input needed to melt the glass composition.

The foregoing and other objects, features, and advantages of the invention will appear more fully hereinafter from a consideration of the detailed description that follows.

DETAILED DESCRIPTION AND PREFERRED EMBODIMENTS

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which the invention belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are described herein. All references cited herein, including published or corresponding U.S. or foreign patent applications, issued U.S. or foreign patents, and any other references, are each incorporated by reference in their entireties, including all data, tables, figures, and text presented in the cited references. The terms “composition” and “formulation” may be used interchangeably herein. Additionally, the phrase “inventive glass composition” and “glass composition” may be interchangeably used.

The present invention relates to a glass composition used to form continuous glass fibers that possess an improved modulus and low density. In some embodiments, the glass composition possesses a low forming temperature and a sufficiently large ΔT to permit the utilization of low-cost refractory tank melters for the formation of the glass fibers instead of conventional high-cost paramelters formed of platinum. By utilizing a refractory tank formed of refractory blocks, manufacturing costs associated with the production of glass fibers produced by the inventive composition are reduced. Additionally, the energy necessary to melt the components of the glass composition is less than the energy necessary to melt many commercially available high performance glass formulations. Such lower energy requirements may also lower the overall manufacturing costs associated with the inventive glass. Further, the composition of the present invention retains the ability to make a commercially acceptable high performance glass fiber and fiber product produced from the glass fibers. In particular, glass fibers formed using the inventive composition may be used to form composite products that are both light weight and exceptionally strong.

The inventive glass composition includes the following components in the weight percent ranges given in Table 1. As used herein, the terms “weight percent” and “percent by weight” may be used interchangeably and are meant to denote the weight percent (or percent by weight) based on the total composition.

TABLE 1 Chemical % by weight SiO₂ 60.0-73.01 Al₂O₃ 13.0-26.0  MgO  5.0-12.75 CaO 0.0-4.0  Li₂O 3.25-4.0  Na₂O 0.0-0.75

In one embodiment, the glass composition comprises SiO₂ in an amount of from about 63.0 to about 73.0% by weight and thus includes the components set forth in Table 1A.

TABLE 1A Chemical % by weight SiO₂ 60.0-73.0 Al₂O₃ 13.0-26.0 MgO  5.0-12.75 CaO 0.0-4.0 Li₂O 3.25-4.0  Na₂O  0.0-0.75

In one embodiment, the glass composition comprises SiO₂ in an amount of from about 63.0 to about 66.0% by weight, Al₂O₃ in an amount of from about 21.0 to about 26.0% by weight, MgO in an amount of from 6.5 to 8.5% by weight, CaO in amount of 0.0 to 2.0% by weight and Li₂O in an amount of 3.25 to 3.5% by weight, and thus includes the components set forth in Table 2.

TABLE 2 Chemical % by weight SiO₂ 63.0-66.0 Al₂O₃ 21.0-26.0 MgO 6.5-8.5 CaO 0.0-2.0 Li₂O 3.25-3.5  Na₂O  0.0-0.75 In this embodiment, the glass composition can comprise SiO₂ in an amount of from about 63.05 to about 65.66% by weight, Al₂O₃ in an amount of from about 21.69 to about 26.0% by weight, MgO in an amount of from 6.88 to 8.49% by weight, CaO in amount of 0.0 to 1.10% by weight, Li₂O in an amount of 3.25 to 3.41% by weight and Na₂O in amount of 0 to 0.75% by weight.

In one embodiment, the glass composition comprises MgO in an amount of from 5.0 to 10.7% by weight, CaO in amount of 0.0 to 23% by weight and Li₂O in an amount of 3.25 to 4.0% by weight, and thus includes the components set forth in Table 3.

TABLE 3 Chemical % by weight SiO₂  63.0-73.01 Al₂O₃ 13.0-26.0 MgO 5.0 to 10.70 CaO 0.0-2.7 Li₂O 3.25-4.0  Na₂O  0.0-0.75 In this embodiment, the glass composition can comprise MgO in an amount of from 5.0 to 10.68% by weight and CaO in amount of 0.0 to 2.66% by weight.

In another embodiment, the glass composition comprises SiO₂ in an amount of from about 60.0 to about 65.5% by weight, CaO in amount of 0.0 to 2.3% by weight and Li₂O in an amount of 3.25 to 3.70% by weight, and thus includes the components set forth in Table 4.

TABLE 4 Chemical % by weight SiO₂ 60.0-65.5 Al₂O₃ 13.0-26.0 MgO  5.0-12.75 CaO 0.0-2.3 Li₂O 3.25-3.7  Na₂O  0.0-0.75

In another embodiment, the glass composition comprises SiO₂ in an amount of from about 60.0 to about 65.5% by weight, CaO in amount of 0.0 to 2.3% by weight and Li₂O in an amount of 3.30 to 3.70% by weight, and thus includes the components set forth in Table 4A.

TABLE 4A Chemical % by weight SiO₂ 60.0-65.5 Al₂O₃ 13.0-26.0 MgO  5.0-12.75 CaO 0.0-2.3 Li₂O 3.30-3.7  Na₂O  0.0-0.75 In this embodiment, the glass composition can comprise SiO₂ in an amount of from about 60.0 to about 65.20% by weight, Al₂O₃ in an amount of 19.33 to 26.00% by weight, MgO in an amount of from 6.88 to 12.75% by weight, CaO in amount of 0.66 to 2.26% by weight, Li₂O in an amount of 3.32 to 3.63% by weight and Na₂O in amount of 0.13 to 0.75% by weight.

In each of the embodiments described above, CaO can be present in an amount of at least 0.1% by weight and/or Na₂O can be present in an amount of at least 0.05% by weight.

Further, impurities or tramp materials may be present in the glass composition without adversely affecting the glasses or the fibers. These impurities may enter the glass as raw material impurities or may be products formed by the chemical reaction of the molten glass with furnace components. Non-limiting examples of tramp materials include potassium, iron, zinc, strontium, and barium, all of which are present in their oxide forms, and fluorine and chlorine. The glass composition of the present invention can be free or substantially free of B₂O₃ and fluorine.

The present invention also relates to glass fibers formed from the inventive glass compositions. Pristine glass fibers (i.e., unsized and untouched laboratory produced fibers) have a fiber tensile strength between about 4390 and about 4820 MPa or between about 4500 and about 4820 MPa. Additionally, the pristine fibers have a modulus between about 82 and about 91 GPa or between about 83 and about 90 GPa. Additionally, the pristine fibers have a density from about 2.39 to about 2.52 g/cc. The fiber tensile strength is also referred to herein as “strength” and is measured on pristine fibers using an Instron tensile testing apparatus according to ASTM D2343-09. As referred to herein, the modulus is an average of measurements on 5 single glass fibers measured in accordance with the procedure outlined in the report, “Glass Fiber and Measuring Facilities at the U.S. Naval Ordnance Laboratory”, Report Number NOLTR 65-87, Jun. 23, 1965. The density is measured by the Archimedes method (ASTM C693-93 (2008)) on unannealed bulk glass.

In one embodiment, the glass fibers have a density of less than 2.477 g/cc. In this embodiment, the glass fibers can be formed from the composition defined in relation to Table 3.

Fiberizing properties of the glass composition of the present invention include the fiberizing temperature, the liquidus temperature, and ΔT. The fiberizing temperature is defined as the temperature that corresponds to a viscosity of about 1000 Poise and as used herein is measured using a rotating cylinder method (ASTM C965-96 (2007)). The fiberizing temperature can also be referred to as the log 3 temperature or the forming viscosity. Lowering the fiberizing temperature may reduce the production cost of the glass fibers because it allows for a longer bushing life and reduced energy usage. For example, at a lower fiberizing temperature, a bushing operates at a cooler temperature and does not quickly “sag”. Sag is a phenomenon that occurs in bushings that are held at an elevated temperature for extended periods of time. Thus, by lowering the fiberizing temperature, the sag rate of the bushing may be reduced and the bushing life can be increased.

In addition, a lower fiberizing temperature allows for a higher throughput since more glass can be melted in a given period at a given energy input. Additionally, a lower fiberizing temperature will permit glass formed with the inventive composition to be melted in a refractory-lined melter instead of conventional high-cost paramelters formed of platinum since both its melting and fiberizing temperatures are below the upper use temperatures of many commercially available refractories. In the present invention, the glass composition has a fiberizing temperature (i.e., log 3 temperature) that is less than about 1505° C. and can be less than 1500° C. or less than about 1400° C. In exemplary embodiments, the log 3 temperature is from about 1280° C. to about 1500° C. or to about 1505° C. In one embodiment, the log 3 temperature is from about 1283° C. to about 1501° C.

The liquidus temperature is defined as the highest temperature at which equilibrium exists between liquid glass and its primary crystalline phase. As used herein the liquidus temperature is measured by exposing the glass composition to a temperature gradient in a platinum-alloy boat for 16 hours (ASTM C829-81 (2005)).

At all temperatures above the liquidus temperature, the glass is free from crystals in its primary phase. At temperatures below the liquidus temperature, crystals may form. Additionally, the liquidus temperature is the greatest temperature at which devitrification can occur upon cooling the glass melt. At all temperatures above the liquidus temperature, the glass is completely molten. The liquidus temperature of the inventive composition is desirably no greater than about 1380 or 1320° C., and may range from about 1230 to about 1380 or from about 1250° C. to about 1320° C.

A third fiberizing property is “ΔT”, which is defined as the difference between the fiberizing temperature (i.e., log 3 temperature) and the liquidus temperature. If the ΔT is too small, the molten glass may crystallize within the fiberizing apparatus and cause an interruption in the manufacturing process. Desirably, the ΔT is as large as possible for a given forming viscosity. A larger ΔT offers a greater degree of flexibility during fiberizing and helps to avoid devitrification both in the glass distribution system and in the fiberizing apparatus. Additionally, a large ΔT reduces the production cost of the glass fibers by allowing for a greater bushing life and a less sensitive forming process. The inventive composition may have a ΔT up to about 205° C., and in exemplary embodiments, from about 28° C. to about 205° C. In one embodiment, the inventive composition may have a ΔT up to about 50° C.

Another property of importance is the specific modulus. Is it desirable to have a specific modulus as high as possible to achieve a lightweight composite material that adds stiffness to the final article. Specific modulus is important in applications where stiffness of the product is an important parameter, such as in wind energy and aerospace applications. In the inventive composition, the glass fibers have a specific modulus from about 34.5 MJ/kg to about 35.9 MJ/kg. In addition, the glass fibers have a specific strength from about 1.8 MJ/kg to about 2.0 MJ/kg.

In one embodiment, the glass fibers have a specific modulus of greater than or equal to 35.5 MJ/kg. In this embodiment, the glass fibers can be formed from the compositions defined in relation to Table 4A. In one embodiment, the glass fibers have a specific modulus of 36.0 MJ/Kg.

In general, glass fibers according to the present invention may be formed by obtaining the raw materials or ingredients and mixing or blending the components in a conventional manner in the appropriate quantities to give the desired weight percentages of the final composition. For example, the components may be obtained from suitable ingredients or raw materials including, but not limited to, sand or pyrophyllite for SiO₂, limestone, burnt lime, wollastonite, or dolomite for CaO, kaolin, alumina or pyrophyllite for Al₂O₃, dolomite, dolomitic quicklime, brucite, enstatite, talc, burnt magnesite, or magnesite for MgO, lithium carbonate or spodumene for Li₂O, and sodium carbonate, sodium feldspar, or sodium sulfate for Na₂O. Glass cullet can also be used to supply one or more of the needed oxides. The mixed batch is then melted in a traditional refractory furnace or melter, and the resulting molten glass is passed along a forehearth and into bushings (e.g., platinum-alloy based bushings) located along the bottom of the forehearth. The operating temperatures of the glass in the furnace, forehearth, and bushing are selected to appropriately adjust the viscosity of the glass, and may be maintained using suitable methods such as control devices. Preferably, the temperature at the front end of the melter is automatically controlled to reduce or eliminate devitrification. The molten glass is then pulled (drawn) through holes or orifices in the bottom or tip plate of the bushing to form glass fibers. The streams of molten glass flowing through the bushing orifices are attenuated to filaments by winding a strand formed of a plurality of individual filaments on a forming tube mounted on a rotatable collet of a winding machine or chopped at an adaptive speed.

The fibers may be further processed in a conventional manner suitable for the intended application. For instance, the glass fibers may be sized with a sizing composition known to those of skill in the art. The sizing composition is in no way restricted, and may be any sizing composition suitable for application to glass fibers. The sized fibers may be used for reinforcing substrates such as a variety of plastics where the product's end use requires high strength and stiffness and low weight. Such applications include, but are not limited to, woven fabrics for use in forming wind blades, armor plating, and aerospace structures. In this regard, the present invention also includes a composite material including the inventive glass fibers, as described above, in combination with a hardenable matrix material. The matrix material may be any suitable thermoplastic or thermoset resin known to those of skill in the art, such as, but not limited to thermoplastics such as polyesters, polypropylene, polyamide, polyethylene terephtalate, and polybutylene, and thermoset resins such as epoxy resins, unsaturated polyesters, phenolics, vinylesters, and elastomers. These resins can be used alone or in combination.

Having generally described this invention, a further understanding can be obtained by reference to certain specific examples illustrated below which are provided for purposes of illustration only and are not intended to be all inclusive or limiting unless otherwise specified.

EXAMPLES Example 1 High Performance Glass Compositions

Glass compositions according to the present invention were made by mixing reagent grade chemicals in proportioned amounts to achieve a final glass composition with the oxide weight percentages set forth in Table 4. The raw materials were melted in a platinum crucible in an electrically heated furnace at a temperature of 1650° C. for 3 hours. The forming viscosity (i.e., the temperature that corresponds to a viscosity of about 1000 Poise) was measured using a rotating cylinder method (ASTM C965-96 (2007)). The liquidus temperature was measured by exposing glass to a temperature gradient in a platinum-alloy boat for 16 hours (ASTM C829-81 (2005)). Density was measured by the Archimedes method (ASTM C693-93 (2008)) on unannealed bulk glass. The modulus reported in the tables below is an average of measurements on 5 single glass fibers measured in accordance with the procedure outlined in the report, “Glass Fiber and Measuring Facilities at the U.S. Naval Ordnance Laboratory”, Report Number NOLTR 65-87, Jun. 23, 1965. The strength was measured on pristine filaments using an Instron tensile testing apparatus (ASTM D2343-09).

TABLE 4 Ex. 1 Ex. 2 Ex. 3 Ex. 4 Ex. 5 Ex. 6 Ex. 7 (% by wt.) (% by wt.) (% by wt) (% by wt.) (% by wt.) (% by wt.) (% by wt.) Chemical SiO₂ 65.20 73.01 63.05 63.68 64.33 65.02 65.04 Al₂O₃ 21.94 16.79 26.00 19.33 20.46 21.64 21.69 MgO 8.21 6.36 6.88 12.75 7.68 8.10 8.12 CaO 1.06 0.45 0.62 0.75 4.00 1.03 1.03 Li₂O 3.37 3.30 3.32 3.34 3.35 4.00 3.37 Na₂O 0.22 0.09 0.13 0.15 0.18 0.21 0.75 Property Forming 1376 1501 1384 1294 1337 1356 1375 Viscosity (° C.) Liquidus 1274 1296 1317 1258 1255 1275 1268 Temperature (° C.) ΔT 102 205 68 35 82 81 107 (° C.) Density 2.4613 2.3916 2.4641 2.5026 2.4893 2.4594 2.4613 (g/cc) Modulus 87.4 82.6 88.5 89.6 87.1 86.5 87.5 GPa Strength 4682 4790 4735 4500 4508 4588 4688 MPa Specific 35.5 34.5 35.9 35.8 35.0 35.2 35.5 Modulus (MJ/kg)

TABLE 5 Ex. 8 Ex. 9 Ex. 10 Ex. 11 Ex. 12 Ex. 13 (% by wt.) (% by wt.) (% by wt.) (% by wt) (% by wt.) (% by wt.) Chemical SiO₂ 60.00 69.44 66.76 65.66 65.24 65.27 Al₂O₃ 23.60 13.00 22.76 22.19 21.97 21.99 MgO 10.07 10.68 5.00 8.49 8.24 8.26 CaO 2.26 2.66 1.65 0.00 1.08 1.10 Li₂O 3.63 3.71 3.50 3.41 3.25 3.38 Na₂O 0.44 0.51 0.33 0.25 0.22 0.00 Property Forming 1283 1302 1443 1390 1375 1376 Viscosity (° C.) Liquidus 1252 1273 1297 1311 1286 1297 Temperature (° C.) ΔT 31 28 146 79 89 79 (° C.) Density 2.5169 2.4704 2.4331 2.4516 2.4631 2.4622 (g/cc) Modulus 90.1 85.7 85.5 86.6 87.3 87.1 GPa Strength 4593 4393 4797 4691 4765 4819 MPa Specific 35.8 34.7 35.1 35.3 35.5 35.4 Modulus (MJ/kg)

Looking at Tables 4 and 5, it can be concluded that the glass compositions of Examples 1-13 have forming viscosity temperatures that are applicable for use in refractory furnaces. In some cases, the specific modulus values for the glasses nearly equal commercial S2 glass manufactured by AGY which has a specific modulus of 36 MJ/Kg as measured by the same method and personnel as these samples. These glasses are especially suited for applications that require stiffness that is equal to that of S2 glass but without the high strength of S2 glass, such as, for example, wind blades. In addition, the density of some of the glasses shown in Tables 4 and 5 is extremely low, which allows these glasses to be employed in aerospace applications. (Cf., AGY S2 at 2.477 g/cc)

The invention of this application has been described above both generically and with regard to specific embodiments. Although the invention has been set forth in what is believed to be the preferred embodiments, a wide variety of alternatives known to those of skill in the art can be selected within the generic disclosure. The invention is not otherwise limited, except for the recitation of the claims set forth below. 

What is claimed is:
 1. A composition for preparing high strength, light weight glass fibers comprising: SiO₂ in an amount from about 60.0 to about 73.01% by weight of the total composition, Al₂O₃ in an amount from about 21.69 to about 26.0% by weight of the total composition, MgO in an amount from about 5.0 to about 12.75% by weight of the total composition, CaO in an amount from 0.1 to about 2.74% by weight of the total composition, Li₂O in an amount from about 3.25 to about 4.0% by weight of the total composition, and Na₂O in an amount from 0.0 to about 0.75% by weight of the total composition, wherein said composition is free of any intentionally added ZnO and wherein said composition has a liquidus temperature no greater than 1380° C.
 2. The glass composition of claim 1, wherein SiO₂ is present in an amount from about 63.0 to about 66.0% by weight of the total composition, Al₂O₃ is present in an amount from about 21.69 to about 26.0% by weight of the total composition, MgO is present in an amount from 6.5 to about 8.5% by weight of the total composition, CaO is present in an amount from about 0.45 to about 2.0% by weight of the total composition, and Li₂O is present in an amount from about 3.25 to about 3.5% by weight of the total composition.
 3. The glass composition of claim 1 wherein, MgO is present in an amount from 5.0 to about 10.70% by weight of the total composition, CaO is present in an amount from about 0.1 to about 2.7% by weight of the total composition, and Li₂O is present in an amount from about 3.25 to about 4.0% by weight of the total composition.
 4. The glass composition of claim 1, wherein SiO₂ is present in an amount from about 60.0 to about 65.5% by weight of the total composition, CaO is present in an amount from about 0.45 to about 2.3% by weight of the total composition, and Li₂O is present in an amount from about 3.25 to about 3.7% by weight of the total composition.
 5. The glass composition of claim 1, wherein said composition is substantially free of B₂O₃ and fluorine.
 6. The glass composition of claim 1, wherein said composition has a ΔT up to about 205° C.
 7. The glass composition of claim 6, wherein said composition has a ΔT from 28° C. to 205° C.
 8. The glass composition of claim 1, wherein said composition has a log 3 temperature from about 1280° C. to about 1505° C.
 9. The glass composition of claim 8, wherein said composition has a log 3 temperature from about 1283° C. to about 1501° C.
 10. The glass composition of claim 1, wherein said composition has a liquidus temperature no greater than about 1320° C.
 11. The glass composition of claim 1, wherein components of said composition are melted in a refractory tank melter.
 12. A continuous high strength, light weight glass fiber produced from a composition according to claim
 1. 13. The glass fiber of claim 12, wherein said glass fiber has a specific modulus from 35 MJ/kg to about 36 MJ/kg and a specific strength from about 1.8 MJ/kg to about 2.0 MJ/kg.
 14. The glass fiber of claim 12 or claim 13, wherein said glass fiber has a pristine fiber tensile strength from about 4390 to about 4820 MPa, a modulus from about 82 to about 90 GPa, and a density from about 2.39 to about 2.52 g/cc.
 15. The glass fiber of claim 14, wherein said glass fiber has a modulus between about 83 and about 90 GPa.
 16. The glass fiber of claim 14, wherein said glass fiber has a density of from 2.39 to less than 2.477 g/cc.
 17. A method of forming a continuous high performance glass fiber comprising: providing a molten glass composition including a composition according to claim 1; and drawing said molten glass composition through orifices in a bushing to form a continuous glass fiber.
 18. The method of claim 17, wherein said glass fiber has a specific modulus from about 34.5 M J/kg to about 35.9 M J/kg and a specific strength from about 1.8 M J/kg to about 2.0 MJ/kg.
 19. The method of claim 17, wherein said glass fiber has a pristine fiber tensile strength from about 4390 to about 4820 MPa, a modulus from about 82 to about 90 GPa, and a density from about 2.39 to about 2.52 g/cc.
 20. The method of claim 18, wherein said glass fiber has a modulus between about 83 and about 90 GPa.
 21. The method of claim 19, wherein said glass fiber has a density of from 2.39 to less than 2.477 g/cc.
 22. A reinforced composite product comprising: a polymer matrix; and a plurality of glass fibers, wherein said glass fibers are according to claim
 12. 23. The composite product of claim 22, wherein said polymer matrix is a thermoplastic polymer selected from polyesters, polypropylene, polyamide, polyethylene terephtalate, polybutylene and combinations thereof.
 24. The composite product of claim 22, wherein said polymer matrix is a thermoset polymer selected from epoxy resins, unsaturated polyesters, phenolics, vinylesters and combinations thereof.
 25. A method of preparing a reinforced composite product comprising preparing a plurality of fibers according to the method of claim 17 and combining said fibers with at least one polymer matrix material. 